TDRP/C8orf42 Antikörper (AA 51-150) (Alexa Fluor 594)

Produktnummer ABIN2810937

Produktdetails anti-TDRP/C8orf42 Antikörper

Target: TDRP/C8orf42 (TDRP) (Testis Development Related Protein (TDRP))

Bindungsspezifität: AA 51-150

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TDRP/C8orf42 Antikörper ist konjugiert mit Alexa Fluor 594

Applikation: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C8orf42

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu TDRP/C8orf42

Target: TDRP/C8orf42 (TDRP) (Testis Development Related Protein (TDRP))

Andere Bezeichnung: C8orf42 (TDRP Produkte)

Synonyme: C8orf42 antikoerper, Inm01 antikoerper, TDRP1 antikoerper, TDRP2 antikoerper, 2610019F03Rik antikoerper, c8orf42 antikoerper, testis development related protein antikoerper, testis development related protein L homeolog antikoerper, TDRP antikoerper, Tdrp antikoerper, tdrp.L antikoerper

Hintergrund:

Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf42 gene product has been provisionally designated C8orf42 pending further characterization.

Subcellular location: Cytoplasm, Nucleus

Synonyms: C8orf42, TDRP_HUMAN, Protein INM01, Protein TDRP, Uncharacterized protein C8orf42.

Gen-ID: 157695